Skeletal diversification via heteroatom linkage control: preparation of bicyclic and spirocyclic scaffolds from N-substituted homopropargyl alcohols. - Wikidata - wikimedia - TriplyDB

Skeletal diversification via heteroatom linkage control: preparation of bicyclic and spirocyclic scaffolds from N-substituted homopropargyl alcohols.

Skeletal diversification via heteroatom linkage control: preparation of bicyclic and spirocyclic scaffolds from N-substituted homopropargyl alcohols.

http://www.wikidata.org/entity/Q34627607

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Synthesis of a family of spirocyclic scaffolds: building blocks for the exploration of chemical space Synthesis of cyclic 1,3-diols as scaffolds for spatially directed libraries Synthesis of Spirocyclic Pyrrolidines: Advanced Building Blocks for Drug Discovery.

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P2860

Skeletal diversification via heteroatom linkage control: preparation of bicyclic and spirocyclic scaffolds from N-substituted homopropargyl alcohols.

http://www.wikidata.org/entity/Q34627607

description

2013 nî lūn-bûn

@nan

2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2013 թվականի ապրիլին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Skeletal diversification via h ...... ituted homopropargyl alcohols.

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Skeletal diversification via h ...... ituted homopropargyl alcohols.

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Skeletal diversification via h ...... ituted homopropargyl alcohols.

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type

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Skeletal diversification via h ...... ituted homopropargyl alcohols.

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Skeletal diversification via h ...... ituted homopropargyl alcohols.

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Skeletal diversification via h ...... ituted homopropargyl alcohols.

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Skeletal diversification via h ...... ituted homopropargyl alcohols.

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Skeletal diversification via h ...... ituted homopropargyl alcohols.

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Skeletal diversification via h ...... ituted homopropargyl alcohols.

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P1433

Journal of Organic Chemistry

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Skeletal diversification via h ...... ituted homopropargyl alcohols.

@en

P2093

Conrad Santini

http://www.w3.org/2001/XMLSchema#string

Frank J Schoenen

http://www.w3.org/2001/XMLSchema#string

Jonathon R Bunn

http://www.w3.org/2001/XMLSchema#string

Justin T Douglas

http://www.w3.org/2001/XMLSchema#string

Thomas O Painter

http://www.w3.org/2001/XMLSchema#string

Victor W Day

http://www.w3.org/2001/XMLSchema#string

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Short synthesis of skeletally and stereochemically diverse small molecules by coupling petasis condensation reactions to cyclization reactions

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Towards the optimal screening collection: a synthesis strategy

Parallel synthesis of a multi-substituted benzo[b]furan library.

Diverging DOS strategy using an allene-containing tryptophan scaffold and a library design that maximizes biologically relevant chemical space while minimizing the number of compounds.

Skeletal diversity via cationic rearrangements of substituted dihydropyrans.

Diversity-oriented synthesis: producing chemical tools for dissecting biology.

Exploring chemical diversity via a modular reaction pairing strategy

Applications of multicomponent reactions for the synthesis of diverse heterocyclic scaffolds.

Synthesis of 2,3-disubstituted benzo[b]furans by the palladium-catalyzed coupling of o-iodoanisoles and terminal alkynes, followed by electrophilic cyclization.

P304

3720-3730

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scholarly article

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10.1021/JO400077M

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P407

P433

8

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78

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2013-04-01T00:00:00Z

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236062637

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23510238

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P932

3691958

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